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Carnosic acid protects against 6-hydroxydopamine-induced neurotoxicity in in vivo and in vitro model of Parkinson's disease: Involvement of antioxidative enzymes induction
被引:86
|作者:
Wu, Chi-Rei
[1
]
Tsai, Chia-Wen
[2
]
Chang, Shu-Wei
[3
]
Lin, Chia-Yuan
[2
]
Huang, Li-Chun
[2
]
Tsai, Chia-Wen
[2
]
机构:
[1] China Med Univ, Coll Pharm, Sch Chinese Pharmaceut Sci & Chinese Med Resource, Taichung, Taiwan
[2] China Med Univ, Dept Nutr, Taichung, Taiwan
[3] Dayeh Univ, Dept Med Bot & Hlth Care, Changhua, Taiwan
关键词:
Carnosic acid;
Neuroprotection;
Antioxidative enzymes;
Apoptosis;
Wistar rats;
GLUTATHIONE METABOLISM;
PC12;
CELLS;
OXIDATIVE STRESS;
SH-SY5Y CELLS;
APOPTOSIS;
6-OHDA;
ACTIVATION;
DEATH;
CONSTITUENTS;
BCL-2/BAX;
D O I:
10.1016/j.cbi.2014.11.011
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The neuroprotective effects of carnosic acid (CA), a phenolic diterpene isolated from rosemary (Rosmarinus officinalis), have been widely investigated in recent years, however, its protection in in vivo still unclear. In this study, we investigated the behavioral activity and neuroprotective effects of CA in a rat model of Parkinson's disease (PD) induced by 6-hydroxydopamine (6-OHDA). Rats were treated with 20 mg/kg body weight of CA for 3 weeks before 6-OHDA exposure. Results indicated that CA improved the locomotor activity and reduced the apomorphine-caused rotation in 6-OHDA-stimulated rats. Significant protection against lipid peroxidation and GSH reduction was observed in the 6-OHDA rats pre-treated with CA. Pretreatment with CA increased the protein expression of gamma-glutamate-cysteine ligase catalytic subunit, gamma-glutamate-cysteine ligase modifier subunit, superoxide dismutase, and glutathione reductase compared with 6-OHDA-stimulated rats and SH-SY5Y cells. Immunoblots showed that the reduction of the Bcl-2/Bax ratio, the induction of caspase 3 cleavage, and the induction of poly(ADPribose) polymerase (PARP) cleavage by 6-OHDA was reversed in the presence of SB203580 (a p38 inhibitor) or SP600125 (a JNK inhibitor) in SH-SY5Y cells. Rats treated with CA reversed the 6-OHDA-mediated the activation of c-JunNH2-terminal kinase and p38, the down-regulation of the Bcl-2/Bax ratio, the up-regulation of cleaved caspase 3/caspase 3 and cleaved PARP/PARP ratio, and the down-regulation of tyrosine hydroxylase protein. However, BAM7, an activator of Bax, attenuated the effect of CA on apoptosis in SH-SY5Y cells. These results suggest that CA protected against 6-OHDA-induced neurotoxicity is attributable to its anti-apoptotic and anti-oxidative action. The present findings may help to clarify the possible mechanisms of rosemary in the neuroprotection of PD. (C) 2014 Published by Elsevier Ireland Ltd.
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页码:40 / 46
页数:7
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